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Modeling of Charge Transfer Induced Spin Transition in a Linear {FeCoFe} Complex

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dc.contributor.author OSTROVSKY, S. M.
dc.contributor.author KLOKISHNER, S. I.
dc.date.accessioned 2020-05-27T20:48:09Z
dc.date.available 2020-05-27T20:48:09Z
dc.date.issued 2019
dc.identifier.citation OSTROVSKY, S. M., KLOKISHNER, S. I. Modeling of Charge Transfer Induced Spin Transition in a Linear {FeCoFe} Complex. In: ICNMBE-2019: International conference on Nanotechnologies and Biomedical Engineering: proc. of the 4rd intern. conf., Sept. 18-21, 2019: Program and Abstract Book. Chişinău, 2019, p. 79. ISBN 978-9975-72-392-3. en_US
dc.identifier.isbn 978-9975-72-392-3
dc.identifier.uri http://repository.utm.md/handle/5014/8424
dc.identifier.uri https://doi.org/10.1007/978-3-030-31866-6_9
dc.description Access full text - https://doi.org/10.1007/978-3-030-31866-6_9 en_US
dc.description.abstract The magnetic behavior of the {[FeTp(CN)3]2Co(Meim)4} • 6H2O compound is examined. Since the observed charge transfer induced spin transition in this compound is accompanied by electronic density redistribution, the theoretical model includes the electron transfer between the Fe and Co ions and two types of cooperative interactions, namely, the electron-deformational and dipole-dipole interactions. It is demonstrated that at low temperatures the spin transformation in the compound under study is accompanied by the appearance of macroscopic polarization. The developed model gives a quite good explanation of the observed effective magnetic moment. en_US
dc.language.iso en en_US
dc.publisher Tehnica UTM en_US
dc.rights Attribution-NonCommercial-NoDerivs 3.0 United States *
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/3.0/us/ *
dc.subject charge transfer en_US
dc.subject macroscopic polarization en_US
dc.subject electrons transfer en_US
dc.subject electron-deformational interactions en_US
dc.subject dipole-dipole interactions en_US
dc.title Modeling of Charge Transfer Induced Spin Transition in a Linear {FeCoFe} Complex en_US
dc.type Article en_US


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